Epidemiological risk assessment using linked network and grid based modelling: Phytophthora ramorum and Phytophthora kernoviae in the UK

We developed a stochastic simulation model incorporating most processes likely to be important in the spread of Phytophthora ramorum and similar diseases across the British landscape (covering Rhododendron ponticum in woodland and nurseries, and Vaccinium myrtillus in heathland). The simulation allows for movements of diseased plants within a realistically modelled trade network and long-distance natural dispersal. A series of simulation experiments were run with the model, representing an experiment varying the epidemic pressure and linkage between natural vegetation and horticultural trade, with or without disease spread in commercial trade, and with or without inspections-with-eradication, to give a 2 × 2 × 2 × 2 factorial started at 10 arbitrary locations spread across England. Fifty replicate simulations were made at each set of parameter values. Individual epidemics varied dramatically in size due to stochastic effects throughout the model. Across a range of epidemic pressures, the size of the epidemic was 5–13 times larger when commercial movement of plants was included. A key unknown factor in the system is the area of susceptible habitat outside the nursery system. Inspections, with a probability of detection and efficiency of infected-plant removal of 80% and made at 90-day intervals, reduced the size of epidemics by about 60% across the three sectors with a density of 1% susceptible plants in broadleaf woodland and heathland. Reducing this density to 0.1% largely isolated the trade network, so that inspections reduced the final epidemic size by over 90%, and most epidemics ended without escape into nature. Even in this case, however, major wild epidemics developed in a few percent of cases. Provided the number of new introductions remains low, the current inspection policy will control most epidemics. However, as the rate of introduction increases, it can overwhelm any reasonable inspection regime, largely due to spread prior to detection.     

Assessing the impact of nano- and micro-scale zerovalent iron particles on soil microbial activities: particle reactivity interferes with assay conditions and interpretation of genuine microbial effects

The effects of nano-scale and micro-scale zerovalent iron (nZVI and mZVI) particles on general (dehydrogenase and hydrolase) and specific (ammonia oxidation potential, AOP) activities mediated by the microbial community in an uncontaminated soil were examined. nZVI (diameter 12.5 nm; 10 mg g⁻¹ soil) apparently inhibited AOP and nZVI and mZVI apparently stimulated dehydrogenase activity but had minimal influence on hydrolase activity. Sterile experiments revealed that the apparent inhibition of AOP could not be interpreted as such due to the confounding action of the particles, whereas, the nZVI-enhanced dehydrogenase activity could represent the genuine response of a stimulated microbial population or an artifact of ZVI reactivity. Overall, there was no evidence for negative effects of nZVI or mZVI on the processes studied. When examining the impact of redox active particles such as ZVI on microbial oxidation-reduction reactions, potential confounding effects of the test particles on assay conditions should be considered.     

An on-farm survey of spatial and temporal stratifications of 17β-estradiol concentrations

17β-estradiol (E2) is a natural estrogenic hormone found in animal manure and urine, which may cause endocrine disruption in sensitive organisms. 17β-Estradiol has been widely detected in the environment, and animal agriculture may be an important source. The objectives of this study were to investigate the potential sources and/or spatial and temporal characteristics contributing to detections of E2 at the farm-scale. Soil cores, segmented into 0.15 m increments, were taken down to the water table from four locations (three potential E2 sources and one control) at or around a swine (Sus scrofa domesticus) farm on five different dates between 2006 and 2007. Estradiol was quantified in the soil-water extracts using liquid chromatography-with tandem mass spectrometry (LC/MS/MS) analysis. Estradiol detections were widespread and found in 128 out of 345 extractions (37%). Concentrations ranged from 0 to 1910 ng L⁻¹ (porewater equivalents). A location that received field application of manure had significantly lower E2 concentrations compared to other locations. Also, the spring 2007 E2 concentrations were significantly higher than all other sample dates, perhaps related to climatic and hydrological events. Results suggested E2 was not directly related to manure sources, but was widespread in this environment. Where E2 was detected, highest concentrations favored the upper profile, while the greatest frequency of detections was in the lower profile and near the water table. Detections of E2 were associated with high organic mater contents in the upper profile and high sand contents in the lower profile. The study suggests that E2 is widespread in some soil environments, raising questions as to the source and mechanisms that facilitate its transport and mobility.     

The performance of passive flow monitors and phosphate accumulating passive samplers when exposed to pulses in external water flow rate and/or external phosphate concentrations

Passive samplers are typically calibrated under constant flow and concentration conditions. This study assessed whether concentration and/or flow pulses could be integrated using a phosphate passive sampler (P-sampler). Assessment involved three 21-day experiments featuring a pulse in flow rate, a pulse of filterable reactive phosphate (FRP) concentration and a simultaneous concentration and flow pulse. FRP concentrations were also determined by parallel grab sampling and the P-sampler calibrated with passive flow monitors (PFMs) and direct measurement of flow rates. The mass lost from the PFM over the deployment periods predicted water velocity to within 5.1, 0.48 and 7.1% when exposed to a flow rate pulse (7.5-50 cm s⁻¹), concentration pulse (5-100 μg P L⁻¹), or both simultaneously. For the P-sampler, good agreement was observed between the grab and passive measurements of FRP concentration when exposed to a pulse in flow (6% overestimation) or concentration (2% underestimation).     

Granulometric and Metal Distributions for Post‐Katrina Surficial Particulate Matter Recovered From New Orleans1

Bhadha, Jehangir H., Casey Schmidt, Robert Rooney, Paul Indeglia, Ruben Kertesz, Elizabeth Bevc, and John Sansalone, 2009. Granulometric and Metal Distributions for Post‐Katrina Surficial Particulate Matter Recovered From New Orleans. Journal of the American Water Resources Association (JAWRA) 45(6):1434‐1447. Abstract: Hurricane Katrina and the resulting failure of the levees that surrounded and protected New Orleans generated a significant detained volume of stormwater within the urban area of New Orleans. Between the inundation resulting from levee failure and eventual pumped evacuation of stormwater from the urban area of New Orleans, a large mass of storm‐entrained particulate matter (PM) was deposited in the inundated areas. This study examined the granulometry and granulometric distribution of metals for post‐Katrina surficial PM deposits recovered from 15 sites (10 inundated and 5 non‐inundated) in New Orleans. Results of this examination were compared to pre‐Katrina data from New Orleans. While post‐Katrina analysis of PM indicates that Pb, Zn, and Cu concentrations for PM are reduced for all sites, inundated sites had higher Cu, Pb, and Zn concentrations for the settleable (～25‐75 μm) and sediment (>75 μm) size fractions. A comparison between total metal concentration and the bioavailable (leachable) fraction for PM reveals that inundated sites had up to 19% higher leachable metal concentration compared to non‐inundated sites. The reduction in PM‐bound total metal concentrations for recovered PM can be explained through a combination of scouring (and therefore change in granulometry from pre‐Katrina) that resulted from transport of suspended PM by storm flows and pumped evacuation; as well as leaching and PM‐based redistribution from extended contact with rainfall and during stormwater detention. New Orleans has been exposed to elevated levels of metals through decades of activities that include vehicular transportation, chemical, industrial, and oil production facilities resulting in higher metal concentrations for urban soil‐residual complexes. As a result, the influent storm flows associated with Katrina as an episodic event cannot solely explain the distribution and fate of PM‐associated metal concentrations.     

Nitrate Dynamics in Two Streams Impacted by Wastewater Treatment Plant Discharge: Point Sources or Sinks?

We examined nitrate processing in headwater stream reaches downstream of two wastewater treatment plant outfalls during low streamflow. Our objectives were to quantify nitrate mass flux before and after effluent discharge and to use field and laboratory techniques to assess the mechanism of nitrate uptake. Microcosm experiments were utilized to determine the location of nitrate processing, and molecular biomarkers were used to detect and quantify microbial denitrification. At one site, downstream nitrate mass flux was significantly (p = 0.01) lower than sum of upstream and wastewater effluent fluxes, indicating rapid stream assimilation of incoming nitrate in the vicinity of the point source. Microcosm experiments supported the theory that nitrate processing occurs in sediments. Molecular assays for denitrifcation‐associated functional genes nosZ, nirS, and nirK, provided evidence that effluent contained enriched denitrifying communities relative to ambient stream water. Nitrate loss at the site with greater uptake was correlated with sulfate loss (p < 0.01; r² = 0.86), suggesting a possible link between sulfate reducing bacteria and denitrifying bacterial communities. Results suggest there is an opportunity to better understand nitrate dynamics in cases where point sources may act as point sinks under specific sets of conditions.     

Supplementation of nitrocompounds in broiler diets: Effects on bird performance,ammonia volatilization and nitrogen retention in broiler manure

A study was conducted to evaluate the effects of dietary nitrocompounds on bird performance, ammonia volatilization, and changes in manure nitrogen (N). A total of 200 one-day-old male chicks (Cobb 500) were used for this study. The chicks were raised in electrically heated battery brooders for 18 days. On day 1, birds were allocated into five treatment groups with four replicated pens: (T1) control, a corn and soybean meal diet (3,100 kcal kg^?1 metabolizable energy (ME) and 21% Crude Protein (CP)); (T2) 16.7 mg kg^?1 nitroethanol (NEL); (T3) 33.3 mg kg^?1 NEL; (T4) 16.7 mg kg^?1 nitropropanol (NPL); and (T5) 33.3 mg kg^?1 NPL. The body weight gain, feed intake and feed efficiency were measured on days 7, 14 and 18. Volatized ammonia (VA) and other N forms were measured at collection and following 2 weeks of incubation at 30°C. Broiler growth was not adversely affected by the nitrocompounds at concentrations up to 33.3 mg kg^?1. The results show that initial manure pH was reduced by adding nitroethanol (NEL) and nitropropanol (NPL) to the diet by 0.2 and 0.5 pH units, respectively. Total VA after 2 weeks was unaffected by dietary treatment. The amounts of uric acid decomposed and ammonia produced were closely balanced in the control sample. However, this balance was significantly different among the manures produced by birds receiving nitrocompound treatments. The inclusion of NEL and NPL resulted in the presence of measurable amounts of Xanthine not found in the control group. This study indicates that supplementation of nitroethanol or nitropropanol into broiler diets up to 33.3 mg kg^?1 influences uric acid degradation and ammonia production in broiler manure while maintaining optimal growth performance.     

Distribution of polybrominated diphenyl ethers in Japanese autopsy tissue and body fluid samples

Brominated flame retardants are components of many plastics and are used in products such as cars, textiles, televisions, and personal computers. Human exposure to polybrominated diphenyl ether (PBDE) flame retardants has increased exponentially during the last three decades. Our objective was to measure the body burden and distribution of PBDEs and to determine the concentrations of the predominant PBDE congeners in samples of liver, bile, adipose tissue, and blood obtained from Japanese autopsy cases. Tissues and body fluids obtained from 20 autopsy cases were analyzed. The levels of 25 PBDE congeners, ranging from tri- to hexa-BDEs, were assessed. The geometric means of the sum of the concentrations of PBDE congeners having detection frequencies >50 % (ΣPBDE) in the blood, liver, bile, and adipose tissue were 2.4, 2.6, 1.4, and 4.3 ng/g lipid, respectively. The most abundant congeners were BDE-47 and BDE-153, followed by BDE-100, BDE-99, and BDE-28+33. These concentrations of PBDE congeners were similar to other reports of human exposure in Japan but were notably lower than concentrations than those reported in the USA. Significant positive correlations were observed between the concentrations of predominant congeners and ΣPBDE among the samples analyzed. The ΣPBDE concentration was highest in the adipose tissue, but PBDEs were distributed widely among the tissues and body fluids analyzed. The PBDE levels observed in the present study are similar to those reported in previous studies in Japan and significantly lower than those reported in the USA.     

Anaerobic degradation of five polycyclic aromatic hydrocarbons from river sediment in Taiwan

This study investigated the anaerobic degradation of five polycyclic aromatic hydrocarbons (PAHs) from Erren River sediment in southern Taiwan. The degradation rates of PAH were in the order: acenaphthene > fluorene > phenanthrene > anthracene > pyrene. The degradation rate was enhanced when the five compounds were present simultaneously in river sediment. Comparison of the PAH degradation rates under three reducing conditions showed the following order: sulfate-reducing conditions > methanogenic conditions > nitrate-reducing conditions. The addition of electron donors (acetate, lactate and pyruvate) enhanced PAH degradation under methanogenic and sulfate-reducing conditions. However, the addition of acetate, lactate or pyruvate inhibited PAH degradation under nitrate-reducing conditions. The addition of heavy metals, nonylphenol and phthalate esters (PAEs) inhibited PAH degradation. Our results show that sulfate-reducing bacteria, methanogen and eubacteria are involved in the degradation of PAH; sulfate-reducing bacteria constitute a major microbial component in PAH degradation. Of the microorganism strains isolated from the sediment samples, we found that strain ER9 expressed the greatest biodegrading ability.     

Enhancement of nitric oxide decomposition efficiency achieved with lanthanum-based perovskite-type catalyst

Direct decompositions of nitric oxide (NO) by La_0.7Ce_0.3SrNiO₄, La_0.4Ba_0.4Ce_0.2SrNiO₄, and Pr_0.4Ba_0.4Ce_0.2SrNiO₄ are experimentally investigated, and the catalysts are tested with different operating parameters to evaluate their activities. Experimental results indicate that the physical and chemical properties of La_0.7Ce_0.3SrNiO₄ are significantly improved by doping with Ba and partial substitution with Pr. NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄ are 32% and 68%, respectively, at 400 °C with He as carrier gas. As the temperature is increased to 600 °C, NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄, respectively, reach 100% with the inlet NO concentration of 1000 ppm while the space velocity is fixed at 8000 hr^?1. Effects of O₂, H₂O_(g), and CO₂ contents and space velocity on NO decomposition are also explored. The results indicate that NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄, respectively, are slightly reduced as space velocity is increased from 8000 to 20,000 hr^?1 at 500 °C. In addition, the activities of both catalysts (La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄) for NO decomposition are slightly reduced in the presence of 5% O₂, 5% CO₂, or 5% H₂O_(g). For durability test, with the space velocity of 8000 hr^?1 and operating temperature of 600 °C, high N₂ yield is maintained throughout the durability test of 60 hr, revealing the long-term stability of Pr_0.4Ba_0.4Ce_0.2SrNiO₄ for NO decomposition. Overall, Pr_0.4Ba_0.4Ce_0.2SrNiO₄ shows good catalytic activity for NO decomposition.

Implications: Nitrous oxide (NO) not only causes adverse environmental effects such as acid rain, photochemical smog, and deterioration of visibility and water quality, but also harms human lungs and respiratory system. Pervoskite-type catalysts, including La_0.7Ce_0.3SrNiO₄, La_0.4Ba_0.4Ce_0.2SrNiO₄, and Pr_0.4Ba_0.4Ce_0.2SrNiO₄, are applied for direct NO decomposition. The results show that NO decomposition can be enhanced as La_0.7Ce_0.3SrNiO₄ is substituted with Ba and/or Pr. At 600 °C, NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄ reach 100%, demonstrating high activity and good potential for direct NO decomposition. Effects of O₂, H₂O_(g), and CO₂ contents on catalytic activities are also evaluated and discussed.